@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP745684.RAOL-rrzAqReTsa4gvlcwM28bG6zHqxrsB61IpIh0pX7g
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP745684.RAOL-rrzAqReTsa4gvlcwM28bG6zHqxrsB61IpIh0pX7g130_head
{
this:
np:hasAssertion
dgn-np:NP745684.RAOL-rrzAqReTsa4gvlcwM28bG6zHqxrsB61IpIh0pX7g130_assertion
;
np:hasProvenance
dgn-np:NP745684.RAOL-rrzAqReTsa4gvlcwM28bG6zHqxrsB61IpIh0pX7g130_provenance
;
np:hasPublicationInfo
dgn-np:NP745684.RAOL-rrzAqReTsa4gvlcwM28bG6zHqxrsB61IpIh0pX7g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP745684.RAOL-rrzAqReTsa4gvlcwM28bG6zHqxrsB61IpIh0pX7g130_assertion
a
np:Assertion
.
dgn-np:NP745684.RAOL-rrzAqReTsa4gvlcwM28bG6zHqxrsB61IpIh0pX7g130_provenance
a
np:Provenance
.
dgn-np:NP745684.RAOL-rrzAqReTsa4gvlcwM28bG6zHqxrsB61IpIh0pX7g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP745684.RAOL-rrzAqReTsa4gvlcwM28bG6zHqxrsB61IpIh0pX7g130_assertion
{
miriam-gene:701
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGN657101eebf40d5ade0eac901260a2cd2
sio:SIO_000628
miriam-gene:701
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP745684.RAOL-rrzAqReTsa4gvlcwM28bG6zHqxrsB61IpIh0pX7g130_provenance
{
dgn-np:NP745684.RAOL-rrzAqReTsa4gvlcwM28bG6zHqxrsB61IpIh0pX7g130_assertion
dcterms:description
"[While some polymorphic base changes were noted in BUB1, BUBR1, and CDC20, no mutations responsible for impairment of the mitotic checkpoint were found in either the HCC cell lines or HCC specimens, which suggests that these genes did not seem to be involved in tumor development in HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:11932908
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP745684.RAOL-rrzAqReTsa4gvlcwM28bG6zHqxrsB61IpIh0pX7g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:32+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}